Viral Vector Stabilization

ABSTRACT

Combining viral vector with surfactant preserves vector infectivity, and surfactant provided an unexpected benefit by protecting viral vector from damage due to transient elevated temperature.

RELATED APPLICATIONS

This application is a divisional of co-pending U.S. Ser. No. 15/781,707 filed 6 Jun. 2018, which is a United States National Stage entry of and asserts priority to PCT/US2017/025727 filed 3 Apr. 2017, which in turn asserts priority from United States provisional patent filing Ser. No. 62/322,452, filed 14 Apr. 2016, the contents of which are here incorporated by reference.

STATEMENT REGARDING FEDERALLY-SPONSORED RESEARCH OR DEVELOPMENT

None

NAMES OF THE PARTIES TO A JOINT RESEARCH AGREEMENT

Not Applicable.

SEQUENCE LISTING

None.

PRIOR DISCLOSURES BY AN INVENTOR

None.

BACKGROUND

Infective viral particles are useful for many medical uses. For example, attenuated virus are useful as vaccines. Similarly, infective (yet often replication deficient) virus are useful as gene therapy vectors to deliver therapeutic transgenes.

The art teaches that infective virus particles are less than perfectly efficient in transfecting host cells. The art teaches that transfection efficiency may be increased by pre-treating the host cells with surfactant.

The art, however, also cautions that surfactant may damage viral particles, and thus reduce their infectivity. The art thus teaches to pre-treat host cells with surfactant immediately before viral vector transfection, yet avoid mixing the viral vector and surfactant and storing for any significant time. The art thus teaches to provide vector and surfactant as physically separate components for therapy.

We thus attempted to quantify the deleterious effect of surfactant on viral vector. To do so, we prepared a viral vector, measured its infectivity, mixed samples of it with surfactant, and stored the preparations under normal vector storage conditions and, to accelerate the deleterious effect of surfactant, at cycled elevated/cooled temperature (a common drug stability technique called “accelerated” stability testing).

BRIEF SUMMARY

We found that, directly contrary to our own expectations and the teachings of the art, surfactant does not reduce vector infectivity. To the contrary, we found that surfactant preserves vector infectivity: vector mixed with surfactant after storage showed higher infectivity than vector not mixed with surfactant. Further, surfactant provided a qualitatively-unexpected benefit, protecting viral vector from damage due to transient elevated temperature.

Our discovery thus for the first time opens the door to several advances in medical treatments. First, we have found a way to protect virus against heat damage by protecting the virus with surfactant. This enables therapeutic virus (e.g., vaccines or gene therapy vectors) to be manufactured, shipped, stored and distributed at higher temperatures than previously thought possible. This lessens the expense of distribution and increases the scope of the area where the virus may be safely distributed to physicians and patients.

Second, our discovery enables virus manufacturers to increase the shelf life of viral treatments. This enables manufacturers to manufacture in larger batch sizes, and may reduce the amount of virus-based medicines which must be discarded as being out-of-date.

BRIEF DESCRIPTION OF THE FIGURES

None

DETAILED DESCRIPTION

We tested the effect of surfactant on virus infectivity and surprisingly found that storage of a virus with surfactant does not in fact impair virus infectivity. To the contrary, our results show surfactant preserves it. This may be seen by our results in several experimental Examples.

Our Examples use The rAd-IFN virus. The rAd-IFN virus is a non-replicating recombinant adenovirus type 5 (Ad5)-based, interferon alpha-2b (IFNα2b) gene transfer vector. It is being developed as e.g., an intravesical treatment for superficial bladder cancer. rAd-IFN is used to deliver the human IFNα2b gene into cells in the urothelial lining of the bladder. The art teaches that on administration, Syn3™ excipient is included in the Admixture formulation immediately before administration to enhance gene transfer into bladder epithelium. We refer to “Admixture” as the final formulation of rAd-IFN in a patient finished dosage form; it contains rAd-IFN vector, Syn3 and final formulation buffer (“FFB”).

Our discussion of these Examples use the following abbreviations:

-   Admixture A mixture of rAd-IFN and Syn3 and FFB representing the     patient dose in Phase III clinical trial of the gene therapy product -   DP Drug Product -   DS Drug Substance -   FFB Final Formulation Buffer, i.e., a sterile buffer suitable for     injection -   IFNα2b interferon alpha-2b -   rAd-IFN A replication deficient recombinant adenovirus type 5 based     interferon alpha-2b gene transfer vector -   RT Room temperature, ˜20 C. -   Syn3 SYN 3 is the polyamide surfactant commercially available from     the Schering-Plought Inc. division of Merck & Co. (Rahway, N.J.) and     having the structure shown:

The art also uses the abbreviation “SYN3” to refer to the synapsin-3 protein, a protein involved in synaptic neurotransmission. We here use the term to refer to the synthetic surfactant, not the naturally-expressed neurotransmitter polypeptide.

-   TS Test sample

Example 15-0029

The aim of this study was to assess the effect of Syn3 DP on potency of the rAd-IFN gene therapy product in rAd-IFN potency assay. At the same time, two storage temperatures (RT and 2-8° C.) of Syn3 DP powder were compared.

We used two samples of Syn3, one stored in RT and one at 2-8° C. This study entailed performing of two rAd-IFN potency assays, each has one TS made from admixture, and a reference standard rAd-IFN from a known quantified batch as a control sample. One assay has the admixture with RT stored Syn3 DP, the other admixture with Syn3 DP stored in the fridge. The potency assay was conducted as known in the art.

We prepared two admixtures made from these samples, and compared them to each other and to reference standard material in a potency assay. Admixture containing 3×10¹¹ vp/ml of rAd-IFN was made and analyzed in a standard rAd-IFN potency assay. Two assays were run, both having ARKz001 as a control sample/reference standard.

Materials and Methods:

We prepared the Admixture as follows:

a) Add 20 ml of sterile water using a 20 ml syringe and 21 G needle to one vial of Syn3 DP sterile powder and gently agitate vial to mix for a couple of minutes. Allow contents to dissolve and bubbles to disappear for 40 minutes at ambient temperature and light. After reconstitution Syn3 DP should be stored at room temperature and must be used within 24 hours. In this study, potency assay is started immediately after sample preparation.

b) Take a vial of rAd-IFN DP (noting the batch number) from ultra-low temperature freezer (−70 C) and thaw at ambient temperature and light with periodic gentle agitation to mix contents while thawing. Once thawed, invert each vial several times to ensure contents are thoroughly mixed.

c) Pipette 2.1 ml of FFB into a 15 ml tube.

d) Withdraw dissolved Syn3 DP using a 10 ml syringe and 21 G needle into a separate container. Pipette 1.4 ml of Syn3 DP to the tube with FFB and invert several times to mix contents.

e) Withdraw the rAd-IFN DP from the vial using 10 ml syringe and a longer 21 G needle. Use a separate container for the virus and pipette 5.3 ml to the admixture tube.

f) Mix well by inverting admixture container several times.

g) Final vp/ml concentration was 3×1011 vp/ml and volume was 8.8 ml.

We then performed the rAd-IFN potency assay. The prepared Admixture (from above) was used as a test sample. To continue to virus dilutions in potency assay, the admixture was diluted 1:6 in GM (1 ml of admixture+5 ml of GM; 5×1010 vp/ml), and then used as normal TS in potency assay. The reference standard material (ARKz001) is treated normally as in a standard procedure. To properly censor the resulting data, before the tests were run, we decided that in case the assays did not have enough passed plates/TS, the results would be given for information only.

Results from these first two analyses are summarized in the following Table. The rAd-IFN in admixture has average relative potency of 1.29 U/vp. Average potency value for rAd-IFN from three assays is 1.28 U/vp.

Potency Results of Admixtures with Differently Stored Syn3

Syn3 U/vp of U/vp of Assay stored at admixture ARKz001 POT-15-037 RT 1.24 1.06 POT-15-038 2-8° C. 1.34  0.94* Average 1.29 *Only one plate passed statistical testing, potency value here for information only.

Our results confirm that storage of Syn3 surfactant at RT does not in fact adversely affect Syn3 by reducing the Potency of admixture made with it; to the contrary, even after storage at RT, Syn3 appears to produce acceptable Potency.

In this first Example, two admixtures containing rAd-IFN were used as test samples in two potency assays. The admixtures were prepared with Syn3 powder stored at RT and in the refrigerator to see if the storage condition of the Syn3 powder might change the potency of the final Admixture. Our data from these assays served as proof that admixture as sample matrix can in fact be analyzed in a standard Potency assay, i.e., that surfactant does not interfere with a Potency assay.

From these first results, our conclusion is that admixture is a suitable sample type for potency assay and that storage in RT or fridge (2-8° C.) are both suitable for Syn3 powder as far as potency of the final admixture is concerned.

Example 15-0029-ADD1

An in-use stability study for Admixture has been done where stability of admixture in four different catheters up to 24 hours has been tested. Surplus admixture at time point zero was frozen as 128×500 μl in ultra-low freezer (below −60° C.). Set of samples handled with a vent-needle is chosen for this study.

Assays used to estimate the stability of stored admixture are infectivity, potency, HPLC, pH and particle size. Total viral particle amount has been analyzed with HPLC instead of OD₂₆₀.

ARKz001 was employed as the control/reference standard sample in both assays and its potency values were within typically seen values. In one potency test, ARKz001 only passed statistical equivalence testing with one plate, so the potency value here is reported for information only. Nevertheless, the potency values from all of the plates were within expected potency values for ARKz001.

The aim of this follow-up work is to provide a baseline measures for a study of stability of rAd-IFN in its “ready-to-use” clinical formulation (as “Admixture”) with diluent (sterile injectable buffer) and surfactant (e.g., Syn3™) when the preparation is thawed and frozen several times over a period of time per Example 15-0035 below.

Sixty-four (64) 500 μl aliquots of vent-needle admixture (prepared for additional testing) will be reserved as test samples in this work. All aliquots are thawed at each time point and three or four vials are taken for analyses. (1 vial for HPLC, 1 vial for particle size, 1 vial for infective titer and potency, 1 vial for pH) All remaining vials are frozen again to below −60° C. All analyses should be done on the same day if possible. If repeat assays are needed, individual vials will be thawed as needed.

Control Samples: Half of the aliquots (64 pcs) as prepared earlier (vent needle, additional testing) are reserved as control samples. These samples are thawed only as needed for each assay, so they will have only one freeze-thaw cycle before analyzing.

Analytical Methods: The analyses in this and Example 15-0035 will be done as presented in this Table. The time point windows are in—AT1.

Stability study set-up Time Infective Particle point HPLC titre Potency size pH 0 M x x x x x 3 M x x x x NA 6 M x x x x NA 9 M x x x x NA 12 M  x x x x x

Thawing Test Samples: The procedure to thaw test samples will be as follows:

(1) At the first time point, take sixty-four (64) vials (test samples) of vent-needle admixture and put them into a separate storage container from the other 64 vials, which are reserved for control samples. Continue with steps a)-d).

(2) At other time points go straight to step a).

a) Take all remaining aliquots that are intended for test samples and thaw them at RT until they melt.

b) Take three aliquots and put them in the fridge until assays can be done (on the same day).

c) Put the rest of the vials back to the ultra-low freezer.

d) Mark down in −AT1 of this plan that the aliquots have been thawed and frozen. Keep the attachment together with sample submission form/ultra-low freezer content logbook for the samples.

Testing is continued up to a year, which means that the test samples will undergo up to four thaws during this study whereas control samples only one.

HPLC is done on the samples, with a concentration of admixture of approximately 3×10¹¹ vp/ml. Infectivity of admixture is determined with flow cytometry; test sample together with the control/reference standard sample are measured in the same assay. Particle size analysis is done according to the dynamic light scattering method. The pH is determined at the last time point, to see if repeated thawing and freezing has affected e.g. microbial growth in the vials.

The results from the assays done at each time point are collected at time=0, 3, 6, 9 and 12 months, along with assays running numbers. There is a window of ±two weeks for the analyses. This study is continued up to 12 months. The results of the assays are compared to time point zero and to the control/reference standard sample that is run at every time point but with less freeze-thaw cycles. The time point zero result should be identical for both the test samples and the control/reference standard sample.

Our results for time t=0 are as follows:

Results for 15-0029-ADD1 Viral Particle Viral Particle % change from % change from % change from concentration Concentration previous Infectivity previous previous Particle Appearance pH (O.D.260) (HPLC) measure Assay measure Potency measure Size Opalescent 7.76 10¹² vp/mL 3.72¹¹ vp/mL N/A 3.73¹⁰ N/A 1.13 U/vp N/A 113 nm colorless (for information NASIU/mL (for information solution, only) only) no visible particles Time = 0

These data confirm that the samples at t=0 have been properly prepared.

Example 15-0035

The aim of this study is to provide in-use stability and biocompatibility data for rAd-IFN in Admixture. From the samples prepared in Example 15-0015 ADD1 (above), sixty-four (64) vials have been be reserved as control samples, which are only thawed as needed for assays upon each time point. The rest of the vials will undergo several sequential freeze-thaw steps as they are all thawed at each time point, the needed vials are removed for analysis and the rest are frozen back.

rAd-IFN is a replication deficient recombinant adenovirus type 5 (rAd5) based gene transfer vector containing human interferon alpha-2b (IFN) gene in expression cassette that replaces E1a, E1b and pIX regions at the 5′ end of adenovirus genome. The vector has been developed for intravesical treatment of non-muscle invasive bladder cancer. It is currently heading towards Phase III clinical trial. Formerly the product was known by the code SCH 721015 but currently it is referred as rAd-IFN.

rAd-IFN vector is used to deliver the human IFNα2b gene into cells in the urothelial lining of the bladder. Before intravesical administration, Admixture is prepared containing appropriate dose of the rAd-IFN drug product in final formulation buffer (FFB) and 1 mg/ml Syn3 excipient which is included in the Admixture formulation to enhance gene transfer into bladder epithelium. This plan describes in-use stability and biocompatibility study protocol for rAd-IFN in admixture by mimicking phase III clinical scenario. The Admixture containing 3×10¹¹ vp/ml (Dose level 2) is exposed various specified delivery components during admixture preparation followed by holding in IntraVia sterile bag, withdrawal into syringes with 1 hour incubation and catheter administration. The study will include sampling at three different time points with four different catheter types:

-   -   Zero time point=Preparation of Admixture into IntraVia sterile         bag followed by withdrawal into syringe, and delivery via four         different types of catheters.     -   Hold 8 h/RT time point=Admixture preparation into IntraVia         sterile bag and holding in the dark at room temperature (RT) for         8 hours followed by 1 hour incubation at RT and ambient light,         withdrawal into syringes followed by 1 hour incubation at RT and         ambient light and delivery via four different types of         catheters.     -   Hold 24 h/+4° C. time point=Admixture preparation into IntraVia         sterile bag and holding at refrigerated conditions (2-8° C.) for         24 hours followed by 1 hour incubation at RT and ambient light,         withdrawal into syringes followed by 1 hour incubation at RT and         ambient light and delivery via four different types of         catheters.         The stability and biocompatibility will be assessed using the         following assays to characterize any changes in appearance, the         physical and chemical characteristics, biological properties and         virus particle concentration and particle size of rAd-IFN in         Admixture:     -   pH (Ph.Eur. 2.2.3)     -   Appearance (USP chapter 790 and Ph.Eur. 2.2.1 visual method, and         Ph:Eur, 2.2.2 modification of method I)     -   Potency assay     -   Infectivity assay     -   HPLC     -   OD₂₆₀     -   Particle size

The admixture components are:

rAd-IFN DP—rAd-IFN-150702, 4.86×10¹¹ vp/ml, stored at Ultra low freezer

Syn3 DP—Lyophilised powder lot 14071, stored at 2-8° C.

rAD-IFN FFB—rAd-IFN Diluent buffer lot FVTc001, stored at 2-8° C.

Aqua Ad Iniectabilia

Schedule for the in-use stability and biocompatibility study is presented in Table II. The prepared Admixture will be divided equally into two 60 ml syringes and will be used for administration of two different catheters. Both catheters are operated at same time by two separate operators. There are no hold step for zero time point, transfer via catheters and sampling will be performed immediately after admixture preparation followed by sample analysis. For the Hold 8 h/RT time point, prepared Admixture in IntraVia bag will be stored in the dark for 8 hours at RT. For the Hold 24 h/+4° C. time point, prepared Admixture in IntraVia bag will be stored for 24 hours at fridge. Both hold time points also include 1 hour incubation in IntraVia bag at RT and ambient light before withdrawal into 60 ml syringes and 1 hour incubation at RT and ambient light in syringes.

TABLE II Schedule for the in-use stability and biocompatibility study Week −2 Week −2 Week 1 Week 1 Week 2 Week 2 Day 1 Day 2 Day 1 Day 2 Day 1 Day 2 Zero Admixture Admixture time point preparation, preparation, Cat1 and Cat2 Cat3 and Cat4 sampling and sampling and analysis analysis Hold Admixture Admixture 8 h/RT preparation, preparation, time point Cat1 and Cat2 Cat3 and Cat4 sampling and sampling and analysis analysis Hold Admixture Cat1 and Cat2 Admixture Cat3 and Cat4 24 h/+4° C. preparation sampling and preparation, sampling and time point analysis analysis

Preparation of Admixture:

The Admixture containing 3×10¹¹ vp/ml (Dose level 2) may be prepared under laminar flow hood as follows:

-   -   1. To obtain a Syn3 solution, add sterile water using a syringe         and needle to a vial of Syn3 powder and gently agitate vial         to mix. Allow contents to dissolve. After reconstitution Syn3         should be used within 24 hours.     -   2. Remove vials of rAd-IFN from the freezer and thaw with         periodic gentle agitation. Once thawed, invert each vial several         times to ensure contents are thoroughly mixed.     -   3. Add Dilution buffer into an empty mixing vessel.     -   4. Withdraw dissolved Syn3 solution and introduce into mixing         vessel containing the Dilution buffer. Invert the vessel several         times to mix contents well.     -   5. Add rAd-IFN to the mixing vessel and mix gently.         We intend to use the following Analytical assays:

Biological activity of rAd-IFN will be assessed by determining potency and infectivity in suitable cell lines. Appearance will be determined and physical and chemical properties will be characterized by measuring pH. Viral particle concentration and size will be determined using high performance liquid chromatography (HPLC), absorbance at 260 nm (OD260) and particle size assays. All methods are qualified/assay qualification is on-going for this product.

After the completion of the single assay the accepted result will be transferred to a result collection form or laboratory notebook which will contain all the results and assay references for this stability study.

Potency: The potency assay models all steps of the therapeutic mechanism of rAD-IFN: infection of cells, expression of IFN and antitumor activity of the product and measures the killing efficacy of rAd-IFN. Interferon sensitive human bladder cancer cells are transduced using multiple dilutions of reference standard and test samples leading to expression of IFNα2b and subsequent cell death. Interferon-sensitive cells may be purchased commercially from several sources, or may be readily prepared or isolated as is well known in the art. See e.g., Howard R. Hubbell et al., Independent sensitivity of Human Tumor Cell Lines To Interferon and Double-Stranded RNA, 44 Cancer Res., 3252 (1984); Lawrence M. Pfeffer et al., Cytoskeletal Association of Human α-Interferon Receptor Complexes In Interferon-Sensitive and -Resistant Lymphoblastoid Cells, 84 P.N.A.S. 3249, 3249 col. 1 (1987). Cell killing efficiency is determined using a colorimetric method measuring dehydrogenase activity of the living cells. The relative potency of the test sample is determined against the reference standard response curve after testing parallelism by equivalence test as outlined in Ph. Eur. 5.3 and USP <1034>. The assay may be performed as described in Viral Vector Assay and Vector, U.S. Patent Application Ser. No. 62/218,810 filed 15 Sep. 2015, incorporated here by reference.

Infectivity: In infectivity assay, cells that support adenovirus replication are infected with different concentrations of adenovirus. After infection, percentage of infected cells is determined with a flow cytometer utilizing a fluorescently conjugated antibody against an adenoviral structural protein. Samples are analysed in parallel with a reference standard and infectivity is given as relative Infectious Units/ml. Result is calculated using Slope Ratio method as outlined in Ph. Eur. 5.3 and USP <1034> The assay may be performed as described in Viral Vector Assay and Vector, U.S. Patent Application Ser. No. 62/218,810 filed 15 Sep. 2015.

pH: pH of rAd-IFN drug products is buffered around pH 7.8 to ensure acceptability for instillation and long term maintenance of the adenovirus function. The desired pH is confirmed by measuring the sample in solution using a standardized pH meter at room temperature. Test is done according to Ph. Eur. 2.2.3 and USP <38>.

Appearance: Appearance (clarity and degree of opalescence, degree of coloration and determination of visible particulates) of adenoviral vector samples is determined according to European Pharmacopoeia (EP) using visual method (EP 2.2.1 visual method and EP 2.2.2 modification of method I) harmonized with United States Pharmacopoeia (USP) chapter 790 guidelines. The assay may be performed as described in Viral Vector Assay and Vector, U.S. Patent Application Ser. No. 62/218,810 filed 15 Sep. 2015.

HPC: HPLC is used to determine total viral particle of rAd-IFN. Working standard (WS) is used to establish a standard curve. The obtained peak areas are plotted against known virus particle concentration of WS (vp/ml). Virus particle concentration of test samples is interpolated from the standard curve and multiplied with dilution factor. Test samples are analysed as duplicates, and results are reported as average result of two replicate samples. The assay may be performed as described in Viral Vector Assay and Vector, U.S. Patent Application Ser. No. 62/218,810 filed 15 Sep. 2015.

OD₂₆₀: Total viral particle concentration of a drug product must reflect the safe and efficacious dose. The concentration of rAd-IFN is determined spectrophotometrically by measuring optical density at 260 nm (OD₂₆₀) in presence of 0.1% SDS. SDS is used to lyse the viral capsid. A conversion factor of 1.1×10¹² particles per absorbance unit at 260 nm is used. This value is based on scientific literature as well as internal findings. Negative control is used to determine background absorbance to be substracted from the results and positive control to confirm the assay performance.

Particle size: Particle size assay is used to monitor possible particle aggregation. The assay is based on dynamic light scattering, where a laser beam is directed to the analyzed sample and the intensity of scattered light is measured from specific detection angle. The smaller the size of soluble particles, the faster the particles movement in the surrounding liquid and the faster the intensity changes of scattered light. Particle size can be calculated based on data obtained from the fluctuations in the light intensity versus time profile. Particle size assay for rAd-IFN may be performed as known in the art.

Summary

Given our examples, one can derive from them a number of therapeutically valuable and commercially valuable applications. These include, for example:

-   -   1. A composition of matter comprising an infective virus in a         therapeutically-effective amount and lyophilized to remove         substantially all water, mixed with a surfactant in an amount         effective to preserve the infectivity of the virus.     -   2. The composition of matter of paragraph 1, wherein the         surfactant is in an amount effective to preserve the infectivity         of the virus during storage at elevated temperature.     -   3. The composition of matter of paragraph 1, wherein the         surfactant comprises Syn3.     -   4. The composition of matter of matter of paragraph 1, wherein         the infective virus functions as a therapeutic vaccine.     -   5. The composition of matter of paragraph 1, wherein the         infective virus functions as a gene therapy vector.

Given our examples, the artisan may readily devise further variants and modifications on our general theme. For example, while our actual experimental examples involve Syn3, other surfactants are known in the art as useful for increasing viral transfection efficiency. Functionally equivalent surfactants are described, for example, in William BENEDICT, Methods and Compositions for Treatment of Interferon-Resistant Tumors, WO 2005/058368 (30 Jun. 2005) at [0054]-[0055].

Similarly, while our actual experiments used replication-deficient virus, we expect our invention would provide the same benefit to replication-competent virus. Similarly, while our actual experiments used adenovirus, we expect our invention would provide similar benefits to other infective virus preparations using other genera of virus (e.g., adeno-associated virus) and other specific viruses (e.g., measles, mumps and rubella attenuated live virus, oral polio, etc.). Indeed, we expect our invention to also be useful for attenuated bacterial vaccines which use bacterium which are live yet inactive (e.g., Rickettsia sp., Salmonella typhi and Bacillus Calmette-Guerin vaccines).

Similarly, certain of our claims require “transient” storage at elevated temperature. We intend this term to cover periods longer than that known in the art to not adversely affect virus vector infectivity, but not permanent or long-term storage; longer than half an hour perhaps, but shorter than a week. We thus intend the coverage of our patent to be defined not by our specific examples discussed here, but by the legal claims and permissible legal equivalents of them. 

1. A composition of matter comprising an infective agent mixed with a surfactant in an amount effective to preserve the infectivity of the agent, lyophilized to remove substantially all water.
 2. The composition of claim 1 wherein the agent comprises an infective virus.
 3. The composition of claim 2 where the virus is replication-deficient.
 4. The composition of matter of claim 1, wherein the surfactant is in an amount effective to preserve the infectivity of the agent at elevated temperature of at least about 2° C.
 5. The composition of matter of claim 4, where the surfactant is in an amount effective to preserve the infectivity of the agent during transient storage at elevated temperature of at least about 2° C.
 6. The composition of matter of claim 1, wherein said agent comprises a live bacillus.
 7. The composition of matter of claim 1, wherein the surfactant comprises NODA.
 8. The composition of matter of matter of claim 2, wherein the infective virus functions as a therapeutic vaccine.
 9. The composition of matter of claim 2, wherein the infective virus functions as a gene therapy vector.
 10. The composition of matter of claim 1, wherein said composition includes a therapeutically-effective amount of said infective agent.
 11. A method of preserving the infectivity of an infective vector, comprising: mixing an infective agent with a surfactant in an amount effective to preserve the infectivity of the agent, removing substantially all water from the mixture, and storing the mixture.
 12. The method of claim 11, where the infective vector comprises infective virus.
 13. The method of claim 12, where the surfactant comprises NODA.
 14. A composition of matter comprising an infective agent and surfactant, the surfactant in an amount effective to preserve the infectivity of the agent, whereby (a) the infectivity of the infective agent combined with the surfactant is at least 100% of (b) the infectivity of the infective agent without surfactant when stored under the same conditions and for the same time.
 15. The composition of matter of claim 14, wherein (a) the infectivity of the infective agent combined with the surfactant is at least 117% of (b) the infectivity of the infective agent without surfactant when stored under the same conditions and for the same time.
 16. The composition of claim 15, wherein (a) the infectivity of the infective agent combined with the surfactant is at least 129% of (b) the infectivity of the infective agent without surfactant when stored under the same conditions and for the same time.
 17. The composition of claim 16, wherein (a) the infectivity of the infective agent combined with the surfactant is at least 142% of (b) the infectivity of the infective agent without surfactant when stored under the same conditions and for the same time.
 18. The composition of claim 14, whereby (a) the infectivity of the infective agent combined with the surfactant is at least 100% of (b) the infectivity of the infective agent without surfactant when stored under the same conditions for at least three months.
 19. The composition of claim 18, whereby (a) the infectivity of the infective agent combined with the surfactant is at least 100% of (b) the infectivity of the infective agent without surfactant when stored under the same conditions for twelve months.
 20. The composition of claim 14, whereby (a) the infectivity of the infective agent combined with the surfactant is at least 100% of (b) the infectivity of the infective agent without surfactant when stored under the same conditions and for the same time, wherein said conditions comprise at least one freeze-thaw cycle.
 21. A method of medical treatment, the method comprising: a. obtaining a cholic acid derivative of Structure I:

wherein R is a hydrophilic moiety, and b. obtaining a virus having infectivity and then c. mixing the virus with the cholic acid derivative to form an admixture, and then d. storing the admixture for at least about two weeks, wherein after said storage the virus retains at least 80% of its initial infectivity, and then e. infecting human cells with the virus to provide to a human a therapeutically-effective medical treatment.
 22. The method of claim 21 wherein R comprises a moiety with a structure selected from the group consisting of:


23. The method of claim 22, wherein the cholic acid derivative is selected from the group consisting of: NODA, Big Chap and 4-(3,7,12-trihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic (isobutyl carbonic) anhydride.
 24. The method of claim 23, wherein the cholic acid derivative comprises NODA.
 25. The method of claim 21, wherein the virus having infectivity comprises an attenuated virus and wherein the therapeutically-effective medical treatment comprises providing a vaccine.
 26. The method of claim 21, wherein the virus having infectivity has a transgene and wherein the therapeutically-effective medical treatment comprises providing a gene therapy.
 27. The method of claim 21, wherein the virus having infectivity comprises adenovirus.
 28. The method of claim 21, wherein the cholic acid derivative comprises NODA, wherein the virus having infectivity comprises adenovirus having a transgene, and wherein the therapeutically-effective medical treatment comprises providing a gene therapy.
 29. The method of claim 21, wherein the cholic acid derivative comprises Big CHAP, wherein the virus having infectivity comprises Type I poliovirus, and wherein the therapeutically-effective medical treatment comprises providing a vaccine.
 30. The method of claim 21, comprising storing the admixture for at least about three months, wherein after said storage the virus retains at least 80% of its initial infectivity.
 31. The method of claim 30, comprising storing the admixture for at least about twelve months, wherein after said storage the virus retains at least 80% of its initial infectivity.
 32. The composition of matter of claim 14, wherein the infective agent comprises a virus.
 33. The composition of claim 32 where the virus is replication-deficient.
 34. The composition of claim 14, wherein the surfactant is in an amount effective to preserve the infectivity of the infective agent at temperature of 2° C.
 35. The composition of matter of claim 14, wherein said infective agent comprises a live bacillus.
 36. The composition of matter of claim 14, wherein the surfactant comprises NODA.
 37. The composition of matter of matter of claim 32, wherein the virus functions as a therapeutic vaccine.
 38. The composition of matter of claim 32, wherein the virus functions as a gene therapy vector.
 39. The composition of matter of claim 38, wherein the virus is replication-deficient and cannot replicate in normal human cells.
 40. The composition of matter of claim 39, wherein the replication-deficient virus comprises nadofaragene firadenovec. 